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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 647966Generated: October 30, 2026

Sodium hydride → HCID 131711265, compound

https://huagongshe.com/reaction/647966

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant2-Phenyl-3-isopropyl-5-hydroxymethyloxazolidineHCID 12566198—
Reactant4-(3-Chloro-6-methylpyrazin-2-yl)morpholineHCID 57062034—
SolventHexamethylphosphoramideHCID 12679—
ProductHCID 131711265HCID 131711265—

Reaction Steps

10.7 g of 2-chloro-3-morpholinyl-5-methyl-pyrazine and 16.6 g of 2-phenyl-3-isopropyl-5-hydroxymethyloxazolidine are dissolved in 130 ml of hexamethylphosphoric acid triamide. 3.6 g of a 50% strength suspension of sodium hydride in paraffin oil are introduced into this solution over the course of 30 minutes at 0°-5° C., whilst stirring. The mixture is then stirred for 1 hour at 0°-5° C. and 24 hours at room temperature. The reaction mixture is then poured onto 500 ml of ice water and extracted by shaking with ether. The ether extracts are washed with water and evaporated in a waterpump vacuum. The residue is taken up in 200 ml of 1 N sulphuric acid and the reaction mixture is stirred for 15 hours at room temperature and then extracted by shaking with ether. The acid aqueous phase is rendered alkaline with concentrated sodium hydroxide solution and is then extracted by shaking with ether. The ether extracts are washed with water, dried over sodium sulphate and evaporated in a waterpump vacuum. The residue crystallises from ether-pentane. 2-(3'-Isopropylamino-2'-hydroxy-propoxy)-3-morpholinyl-5-methyl-pyrazine, melting point 77°-78° C., is thus obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04410530
Source datasetuspto-grants-1983_10
ORD IDord-e46afa4786824886995de4b7ec330690
Source noteuspto-grants-1983_10